Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2869967
rs2869967
0.820 GeneticVariation BEFREE The FAM13A rs2869967 was associated with COPD (minor CC genotype: P = 0.0007, OR = 2.414). 26310313

2015

dbSNP: rs2869967
rs2869967
C 0.820 GeneticVariation GWASCAT Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. 25241909

2014

dbSNP: rs2869967
rs2869967
0.820 GeneticVariation BEFREE Significant differences in genotypic distributions (χ(2)=6.319, p=0.042 for rs2869967</span>; χ(2)=6.062, p=0.048 for rs3821104) and allele distributions (χ(2)=4.014, p=0.045 for rs2869967; χ(2)=5.607, p=0.018 for rs3821104) were observed between patients and control subjects for variants rs2869967 and rs3821104, whereas no statistically significant associations for genotypic and allelic distribution between IREB2 rs2568494 and COPD phenotype (p>0.05) were identified. 22027142

2011

dbSNP: rs2869967
rs2869967
0.820 GeneticVariation GWASDB Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748

2010